Canonical Allele Identifier: CA2720596686

Gene: RXRA

Linked Data

• dbSNP Id: rs2119157850

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408302_134408312del , CM000671.2:g.134408302_134408312del	GRCh38
NC_000009.11:g.137300148_137300158del , CM000671.1:g.137300148_137300158del	GRCh37
NC_000009.10:g.136439969_136439979del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+3_430+13del MANE Select	ENSP00000419692.1:n.430+3_430+13del
ENST00000672570.1:c.349+3_349+13del	ENSP00000500402.1:n.349+3_349+13del
ENST00000356384.4:n.840+3_840+13del
ENST00000481739.1:c.430+3_430+13del	ENSP00000419692.1:n.430+3_430+13del
NM_001291920.1:c.349+3_349+13del	NP_001278849.1:n.349+3_349+13del
NM_001291921.1:c.139+3_139+13del	NP_001278850.1:n.139+3_139+13del
NM_002957.5:c.430+3_430+13del	NP_002948.1:n.430+3_430+13del
NM_002957.6:c.430+3_430+13del MANE Select	NP_002948.1:n.430+3_430+13del
NM_001291921.2:c.139+3_139+13del	NP_001278850.1:n.139+3_139+13del
NM_001291920.2:c.349+3_349+13del	NP_001278849.1:n.349+3_349+13del